Canonical Allele Identifier: CA2497334623

Gene: MMP1 WTAPP1

Linked Data

• dbSNP Id: rs1858010574

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102790905_102790906insAGCACATGAC , CM000673.2:g.102790905_102790906insAGCACATGAC	GRCh38
NC_000011.9:g.102661636_102661637insAGCACATGAC , CM000673.1:g.102661636_102661637insAGCACATGAC	GRCh37
NC_000011.8:g.102166846_102166847insAGCACATGAC	NCBI36
NG_011740.1:g.12330_12331insGTCATGTGCT
NG_011740.2:g.12330_12331insGTCATGTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315274.7:c.1197-100_1197-99insGTCATGTGCT (MMP1) MANE Select	ENSP00000322788.6:n.1197-100_1197-99insGTCATGTGCT
ENST00000680179.1:n.375-100_375-99insGTCATGTGCT (MMP1)
ENST00000681445.1:n.371-100_371-99insGTCATGTGCT (MMP1)
ENST00000681643.1:n.397-100_397-99insGTCATGTGCT (MMP1)
ENST00000315274.6:c.1197-100_1197-99insGTCATGTGCT (MMP1)	ENSP00000322788.6:n.1197-100_1197-99insGTCATGTGCT
ENST00000371455.7:n.325-7119_325-7118insAGCACATGAC (WTAPP1)
ENST00000525739.6:n.390-2240_390-2239insAGCACATGAC (WTAPP1)
ENST00000544704.1:n.344+6841_344+6842insAGCACATGAC (WTAPP1)
NM_001145938.1:c.999-100_999-99insGTCATGTGCT (MMP1)	NP_001139410.1:n.999-100_999-99insGTCATGTGCT
NM_002421.3:c.1197-100_1197-99insGTCATGTGCT (MMP1)	NP_002412.1:n.1197-100_1197-99insGTCATGTGCT
NR_038390.1:n.390-2240_390-2239insAGCACATGAC (WTAPP1)
NM_002421.4:c.1197-100_1197-99insGTCATGTGCT (MMP1) MANE Select	NP_002412.1:n.1197-100_1197-99insGTCATGTGCT
NM_001145938.2:c.999-100_999-99insGTCATGTGCT (MMP1)	NP_001139410.1:n.999-100_999-99insGTCATGTGCT